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Molecular pathogenesis of long QT syndrome type 1
Long QT syndrome type 1 (LQT1) is a subtype of a congenital cardiac syndrome caused by mutation in the KCNQ1 gene, which encodes the α-subunit of the slow component of delayed rectifier K(+) current (I(Ks)) channel. Arrhythmias in LQT1 are characterized by prolongation of the QT interval on ECG, as...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063268/ https://www.ncbi.nlm.nih.gov/pubmed/27761162 http://dx.doi.org/10.1016/j.joa.2015.12.006 |